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Two-Step Synthesis of 2,3-Dihydropyrroles via a Formal 5-endo Cycloisomerization of Ugi 4-CR/Propargyl Adducts

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Since 1995 the new chemistry of multicomponent reactions and their libraries, including their heterocyclic chemistry

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A facile synthesis of 4-aryl-2,3-dihydropyrroles

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Novel three-component synthesis and antiproliferative properties of diversely functionalized pyrrolines

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Ruthenium Catalyzed Decarbonylative Arylation at sp3 Carbon Centers in Pyrrolidine and Piperidine Heterocycles

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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Indium( III ) chloride

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Indium( III ) chloride

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ChemInform Abstract: Two‐Step Synthesis of 2,3‐Dihydropyrroles via a Formal 5‐endo Cycloisomerization of Ugi 4‐CR/Propargyl Adducts.

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A Passerini/Michael Pathway towards Butyrolactones

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Effect of ortho -substitution on persulfate-mediated decarboxylation and functionalization of arylacetic acids

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Asymmetric synthesis of 4,5-dihydropyrrole derivatives via DKR: DROC of activated aziridines with enaminones

inferred← citeshttps://doi.org/10.1055/a-2005-5220openalex-snapshot

A Mn(OAc)3-Triggered Formation of Cyclopropanes from Ugi Adducts

inferred← citeshttps://doi.org/10.1080/00397911.2016.1152372openalex-snapshot

Synthesis of novel tetrahydroindeno[1,2-b]pyrrolidines via Ugi multicomponent and palladium-catalyzed aerobic oxidative cyclization

inferred← citeshttps://doi.org/10.1107/s2414314619002207openalex-snapshot

(Z)-1-Benzoyl-5-benzylidene-2-hydroxy-4-oxo-4,5-dihydro-1H-pyrrole-3-carbonitrile

inferred← citeshttps://doi.org/10.3389/fchem.2019.00020openalex-snapshot

Raising the Diversity of Ugi Reactions Through Selective Alkylations and Allylations of Ugi Adducts

inferred← citeshttps://doi.org/10.3390/molecules29112486openalex-snapshot

Are Terminal Alkynes Necessary for MAO-A/MAO-B Inhibition? A New Scaffold Is Revealed

inferred← citeshttps://doi.org/10.6023/cjoc202012040openalex-snapshot

Ugi Four-Component Reaction Based on thein situCapture of Amines and Subsequent Modification Tandem Cyclization Reaction: "One-Pot" Synthesis of Six- and Seven-Membered Heterocycles

inferred← citeshttps://doi.org/10.70675/3a6cf4a1zef65z490ez8ad7z88297b83ec7copenalex-snapshot

Multicomponent Reactions toward Heterocycles and Tsuji-Trost Reaction of Allylic Nitro Derivatives

inferred← citeshttps://doi.org/10.70675/9071af9az39a7z4d1ez84f1z07acae47d714openalex-snapshot

Multicomponent reactions for the synthesis of some nitrogenous heterocyclic compounds and studies of their biological activities

inferred← citeshttps://doi.org/10.70675/e41a0f59ze070z4e1ez9fecz5e15f76b97c8openalex-snapshot

Réactions multicomposant à base des isonitriles

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